GM-CSF

GM-CSF granulocyte-macrophage colony-stimulating factor.

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Granulocyte/macrophage colony stimulating factor (GM-CSF)

A substance produced by cells of the immune system that stimulates the attack upon foreign cells. Used to treat prostate cancers as a genetically engineered component of a vaccine that stimulates the body to attack prostate tissue.

Mentioned in: Prostate Cancer

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GM-CSF,

abbreviation for granulocyte-macrophage colony-stimulating factor.

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GM-CSF

granulocyte-macrophage colony-stimulating factor.

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sargramostim (GM-CSF)

Leukine

Pharmacologic class: Granulocyte-macrophage colony stimulating factor

Therapeutic class: Hematopoietic agent

Pregnancy risk category C

Action

Stimulates proliferation and differentiation of hematopoietic cells that activate mature granulocytes and macrophages of target cells

Availability

Liquid: 500 mcg/ml

Powder for injection: 250 mcg

⊘Indications and dosages

➣ Post peripheral blood progenitor cell (PBPC) transplantation

Adults: 250 mcg/m²/day I.V. over 24 hours or subcutaneously once daily, starting immediately after progenitor cell infusion

➣ Mobilization of PBPCs into peripheral blood for collection by leukapheresis

Adults: 250 mcg/m²/day I.V. over 24 hours or subcutaneously once daily, continued throughout harvesting

➣ Neutrophil recovery after chemotherapy in acute myelogenous leukemia

Adults: 250 mcg/m²/day I.V. over 4 hours, starting 4 days after completion of chemotherapy induction

➣ Bone-marrow transplantation failure or engraftment delay

Adults: 250 mcg/m²/day as 2-hour I.V. infusion for 14 days. If engraftment doesn't occur, may repeat after 7 days of drug hiatus.

➣ Myeloid reconstitution after autologous or allogeneic bone-marrow transplantation

Adults: 250 mcg/m²/day as a 2-hour I.V. infusion, starting 2 to 4 hours after autologous bone marrow infusion and at least 24 hours after last chemotherapy or radiotherapy dose

Off-label uses

• Crohn's disease
• Melanoma
• Wound healing
• Mucositis
• Stomatitis
• Vaccine adjuvant

Contraindications

• Hypersensitivity to drug, its components, or yeast products
• Excessive leukemic myeloid blasts in bone marrow or peripheral blood (10% or more)
• Within 24 hours before or after chemotherapy or radiation therapy

Precautions

Use cautiously in:
• renal or hepatic insufficiency, fluid retention, pulmonary disorders, pulmonary infiltrates, heart failure, leukocytosis, transient supraventricular arrhythmias
• cancer patients undergoing sargramostim-mobilized PBPC collection
• patients receiving purged bone marrow or previously exposed to intensive chemotherapy or radiation therapy
• pregnant or breastfeeding patients
• children.

Administration

☞ Don't give within 24 hours of chemotherapy or radiation therapy.
• Add 1 ml of sterile water to powder for injection by directing water stream against side of vial and swirling vial gently to disperse contents.
• Avoid shaking or agitating solution.
• For a final drug concentration below 10 mcg/ml, add human albumin 0.1% to saline solution; then dilute drug in normal saline solution.
• Infuse as soon as possible after reconstitution, but no more than 6 hours after mixing.
• Don't add other drugs to infusion; don't use in-line filter.

Route	Onset	Peak	Duration
I.V.	Immediate	2 hr	3-6 hr
Subcut.	15 min	1-3 hr	6 hr

Adverse reactions

CNS: malaise, asthenia

CV: peripheral edema, tachycardia, hypotension, transient supraventricular tachycardia, pericardial effusion

GI: nausea, vomiting, diarrhea, anorexia, stomatitis, GI hemorrhage

GU: urinary tract disorder, abnormal renal function

Hematologic: blood dyscrasias, hemorrhage

Hepatic: hepatic damage

Musculoskeletal: joint pain, myalgia, bone pain

Respiratory: dyspnea, lung disorder

Skin: rash, alopecia

Other: fever, chills, sepsis, edema, first-dose reaction (respiratory distress, hypoxia, syncope, tachycardia, hypotension, flushing)

Interactions

Drug-drug. Corticosteroids, lithium: potentiation of myeloproliferative effects

Vincristine: severe peripheral neuropathy

Patient monitoring

• Monitor for dyspnea. Halve dosage and contact prescriber if dyspnea occurs.
• Assess CBC with white cell differential. Check for presence of blast cells, and watch for signs and symptoms of blood dyscrasias.
• Closely monitor vital signs and fluid intake and output. Stay alert for signs and symptoms of fluid overload.
☞ Monitor liver function tests, and watch for evidence of hepatic damage and bleeding (especially GI hemorrhage).

Patient teaching

☞ Tell patient sargramostim is a powerful drug that can cause significant adverse reactions. Teach him to recognize and report serious reactions at once.
☞ Instruct patient to immediately report unusual bleeding or bruising or yellowing of skin or eyes.
• Tell patient drug may cause weakness and musculoskeletal pain.
• Inform patient that he'll undergo regular blood testing during therapy.
• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs mentioned above.

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GM-CSF

Granulocyte macrophage-colony stimulating factor, sargramostim, Leukine, Prokine A hematopoietic growth factor and immune modulator produced by granulocytes, macrophages, monocytes, lymphocytes, fibroblasts, endothelial cells; rGM-CSF–sargramostim may be used to ↑WBCs in AIDS, or stimulate hematopoiesis after high dose chemotherapy in autologous BMT; it may be used as an immune 'tonic' in CA and AIDS Pts, anemia, ↑ survival of BMTs, ↓ infections in congenital neutropenia Adverse effects Bone pain, rash, fever. See Biological response modifiers, Sargramostim. Cf G-CSF.